BEUDAMED
    8 results · 7ms · Sources: EU EUDAMED, US FDA

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    Filters Classification: FDA Class 3 ×

    Pulse-Generator, Program Module

    FDA Pre-Market Approval
    FDA Class 3 ·AORTIC VALVULOPLASTY BALLOON DILATATION CATHETER

    Pulse-Generator, Program Module

    FDA Pre-Market Approval
    FDA Class 3 ·AORTIC VALVULOPLASTY BALLOON DILATATION CATHETER

    Pulse-Generator, Program Module

    FDA Pre-Market Approval
    FDA Class 3 ·AORTIC VALVULOPLASTY BALLOON DILATATION CATHETER

    Pulse-Generator, Program Module

    FDA Pre-Market Approval
    FDA Class 3 ·MANSFIELD SCI. AORTIC VALVULOPLASTY CATHETER

    Pulse-Generator, Program Module

    FDA Pre-Market Approval
    FDA Class 3 ·BOSTON SCITNTIFIC SCIMED AORTIC VALVULOPLASTY(TM) CATHETER

    Pulse-Generator, Program Module

    FDA Pre-Market Approval
    FDA Class 3 ·MANSFIELD SCI. AORTIC VALVULOPLASTY CATHETER

    Pulse-Generator, Program Module

    FDA Pre-Market Approval
    FDA Class 3 ·MANSFIELD SCI. AORTIC VALVULOPLASTY CATHETER

    Pulse-Generator, Program Module

    FDA Pre-Market Approval
    FDA Class 3 ·MANSFIELD SCI. AORTIC VALVULOPLASTY CATHETER